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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35250생성일: 2026년 10월 23일

Homoveratrylamine → N-[2-(3,4-dimethoxyphenyl)ethyl]-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide

https://huagongshe.com/ko/reaction/35250

반응식

참여 물질

역할이름HCID투입량
반응물HomoveratrylamineHCID 8421—
반응물Isobutyl chloroformateHCID 62365—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물HCID 178482013HCID 178482013—
용매TetrahydrofuranHCID 8028—
생성물N-[2-(3,4-dimethoxyphenyl)ethyl]-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramideHCID 5405021841%

반응 단계

4-(1-Methyl-1,2,3,4-tetrazol-5-yl)thio-butyric acid (45 mmole) is dissolved in tetrahydrofuran (50 ml), and thereto is added DBU (50 mmole). To the mixture is added dropwise with stirring isobutyl chloroformate (50 mmole) under ice-cooling and the mixture is stirred at room temperature for 30 minutes. To the mixture is added dropwise 2-(3,4-dimethoxyphenyl)ethylamine (54 mmole) and the mixture is further stirred at room temperature for 2 hours. After the solvent is distilled off under reduced pressure, the resulting residue is extracted with chloroform. The chloroform layer is washed with 5% aqueous hydrochloric acid, an aqueous saturated sodium hydrogen carbonate solution and an aqueous saturated sodium chloride solution and dried over anhydrous sodium sulfate. After distilling off chloroform, the residue is subjected to column chromatography (Wakogel C-200, eluting agent, chloroform) to isolate N-[2-(3,4-dimethoxyphenyl)ethyl]-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide (yield: 41%) which is recrystallized from hexane-chloroform, colorless flaks, m.p. 70.5°-71.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04766120
출처 데이터셋uspto-grants-1988_08
ORD IDord-4a703fea81f6423fa60176b3220e22fe
출처 메모uspto-grants-1988_08